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Leprosy Active Searching Trial in Brazil (LAST•Br)

H

Hospital Alemão Oswaldo Cruz

Status

Enrolling

Conditions

Leprosy

Treatments

Other: Implementing active-case finding strategies

Study type

Interventional

Funder types

Other

Identifiers

NCT06761469
78510724.3.0000.0070

Details and patient eligibility

About

The goal of this clinical trial is to assess whether a multifactorial active case-finding strategy improves the detection of leprosy cases in Brazil compared to usual screening practices. The main questions it aims to answer are:

  • Does the intervention increase the number of new leprosy cases detected compared to standard care?

Participants will:

  • Receive community awareness about leprosy.
  • Be screened using the Leprosy Suspicion Questionnaire at priority areas identified by georeference tools.
  • Undergo clinical evaluation by a trained medical team.
  • If leprosy is diagnosed, affected patients will collect complementary laboratory exams

Healthcare professionals from primary care units will receive training in leprosy, while researchers will monitor changes in leprosy incidence over a 12-month period using data from Brazil's national notification system. The study will provide insights into underdiagnosis and the clinical profiles of patients who have been diagnosed.

Enrollment

1,925 estimated patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

(I) Municipalities

  • Municipality recognized by the Brazilian Institute of Geography and Statistics as part of the Brazilian Federation.
  • Municipality with operational epidemiological classification by the Ministry of Health (BMoH) as: 'municipalities with cases in the period from 2015 to 2019'.
  • Municipality with authorization/consent from the government to participate in the study.

(II) Primary Health Units (Unidade Básica de Saúde or UBS) • UBS with territorial coverage (linked population) within the participating municipality.

(III) Participants

• Patients with positive Leprosy Suspicion Questionnaire (LSQ): children under five years old with Free and Informed Consent Form (ICF) signed by parents/guardians, 5-17 years old with ICF signed by parents/guardians and Free and Informed Assent Form (IAF) signed by the minor, and patients over 18 years old with ICF signed for: rapid test collection, comorbidity questionnaire and clinical evaluation; and if leprosy diagnosis is confirmed, collection of complementary exams.

Exclusion criteria

(I) Municipalities

  • Municipality with extreme population size (municipalities with a number of inhabitants lower than the 10th percentile and higher than the 90th percentile).
  • Municipality with operational epidemiological classification by the BMoH as: 'municipalities without cases in the period 2015 to 2019'.
  • Municipalities with active or recent participation (less than one year) in other active-finding strategies, in addition to the usual ones: ministerial, Non-Governmental Organizations (NGOs), academic, among others.

(II) Primary Health Units

  • UBS with limited multidisciplinary team (absence of physicians, nurse and/or community health agents).
  • UBS with difficult access (no access by land, i.e. riverside populations).
  • UBS with territorial coverage exclusively of indigenous populations.

(III) Participants

  • LSQ negative.
  • Patients with a previous diagnosis or history of treated leprosy.
  • Patients residing/registered outside the selected municipality.

Trial design

Primary purpose

Screening

Allocation

Non-Randomized

Interventional model

Sequential Assignment

Masking

None (Open label)

1,925 participants in 2 patient groups

Multifaceted intervention
Experimental group
Description:
Implementation of active-case finding strategies
Treatment:
Other: Implementing active-case finding strategies
Standard of care
No Intervention group
Description:
Routine screening

Trial contacts and locations

1

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Central trial contact

Katia C Braz; Sebastian A Vernal, MD, PhD

Data sourced from clinicaltrials.gov

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